Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference20 articles.
1. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism;Bonifati;Science,2003
2. Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis;Crompton;Mol. Genet. Metab.,2010
3. FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome;Di Fonzo;Neurology,2009
4. Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism;Guo;J. Neurol.,2010
5. Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism;Guo;Neurol. Sci.,2011
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